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sodium tetracarbonyl(triphenyl phosphite)manganate(-I) | 59778-90-4

中文名称
——
中文别名
——
英文名称
sodium tetracarbonyl(triphenyl phosphite)manganate(-I)
英文别名
——
sodium tetracarbonyl(triphenyl phosphite)manganate(-I)化学式
CAS
59778-90-4
化学式
C22H15MnO7P*Na
mdl
——
分子量
500.258
InChiKey
OOENFUSUHBGBMX-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Interfacial Electron Transfer to the Zeolite-Encapsulated Methylviologen Acceptor from Various Carbonylmanganate Donors. Shape Selectivity of Cations in Mediating Electron Conduction through the Zeolite Framework
    摘要:
    The series of (one-electron) reductions of methylviologen (MV(2+)) intercalated into zeolite-Y by various carbonylmanganate donors [C+Mn(CO)(4)L(-), L = CO, P(OPh)(3)] are very selective and highly dependent on the size/ shape of the counterion C+, although the same electron transfers carried out (homogeneously) in solution always occur spontaneously, irregardless of C+. For example, the complete reduction of MV(2+) extensively doped into zeolite-Y proceeds rapidly and quantitatively when the Na+ salts of the carbonylmanganates are employed as the reductants, but only to a very limited extent (1%) when the large PPN+ [bis(triphenylphosphine)iminium] salts of the carbonylmanganates are employed. The medium-size tetraethylammonium (TEA(+)) salt of Mn(CO)(4)P(OPh)(3)(-) slowly effects an intermediate conversion (80%). Based on the fact that the large phosphite-substituted Mn(CO)(4)P(OPh)(3)(-) donor cannot enter the supercage of zeolite-Y, we propose interfacial electron transfer from the carbonylmanganate to the MV(2+) acceptor to occur only at the zeolite periphery. Importantly, the strong dependence of the further progress of the redox reaction with decreasing size of the cation C+ (i.e., shape selectivity) predicts that electron conduction throughout the zeolite framework requires the simultaneous transport of these cations in order to effect the complete reduction of all the encapsulated MV(2+), as presented in Chart 5.
    DOI:
    10.1021/ja962645y
  • 作为产物:
    参考文献:
    名称:
    通过离子对an灭形成金属键。来自锰酸根(I-)阴离子和锰(I)阳离子的二锰羰基羰基化合物
    摘要:
    DOI:
    10.1021/om00152a010
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